Product Details

SNP ID: rs1800035
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:111078794 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGGGGGGCACCGAGCGCAGGCCCAA[C/G]GGTCTGGGCCCCGAGCGCAGCGCGG
Phenotype: MIM: 104210
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: ADRA2A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000681.3	1763	Missense Mutation	AAC,AAG	N266K	NP_000672.3